Retroperitoneal fibrosis
ICD-10 K68.2 is a billable code used to indicate a diagnosis of retroperitoneal fibrosis.
Retroperitoneal fibrosis is a rare condition characterized by the formation of fibrous tissue in the retroperitoneal space, which can lead to obstruction of the ureters and other vital structures. Clinically, patients may present with abdominal or flank pain, renal impairment, and urinary symptoms due to ureteral obstruction. The condition can be idiopathic or secondary to medications, infections, or malignancies. The anatomy involved primarily includes the kidneys, ureters, and surrounding vascular structures. Disease progression can lead to significant renal dysfunction if left untreated, necessitating timely intervention. Diagnostic considerations include imaging studies such as CT or MRI, which can reveal the extent of fibrosis and any associated complications. Laboratory tests may also be performed to assess renal function and rule out other causes of symptoms. Early diagnosis and management are crucial to prevent irreversible damage to the urinary system.
Standard ICD-10-CM documentation requirements apply
Various clinical presentations within this specialty area
Follow specialty-specific billing guidelines
Standard ICD-10-CM documentation requirements apply
Various clinical presentations within this specialty area
Follow specialty-specific billing guidelines
K68.2 specifically covers retroperitoneal fibrosis, which may be idiopathic or secondary to other conditions such as malignancies or certain medications. It is essential to document the underlying cause if known.
K68.2 should be used when there is a confirmed diagnosis of retroperitoneal fibrosis, particularly when imaging studies support the diagnosis and other conditions have been ruled out.
Documentation should include imaging reports (CT or MRI), clinical symptoms, laboratory results indicating renal function, and any relevant medical history that may contribute to the diagnosis.
